With supporting calculations on numerous possible close-lying electronic states, we suggest a potential description of the strong photoelectron-valence electron interactions that may result in the photon-energy-dependent changes in the observed spectra.Chalcogenide-based anodes are receiving increasing attention for rechargeable potassium-ion batteries (PIBs) due to their high theoretical capacities. 6-Benzylaminopurine clinical trial However, they usually exhibit poor electrochemical performance due to poor structural stability, low conductivity, and severe electrolyte decomposition on the reactive surface. Herein, a method analogous to "blowing bubbles with gum" is used to confine FeS2 and FeSe2 in N-doped carbon for PIB anodes with ultrahigh cyclic stability and enhanced rate capability (over 5000 cycles at 2 A g-1). Several theoretical and experimental methods are employed to understand the electrodes' performance. The density functional theory calculations showed high affinity for potassium adsorption on the FeS2 and FeSe2. The in situ XRD and ex situ TEM analysis confirmed the formation of several intermediate phases of the general formula KxFeS2. These phases have high conductivity and large interlayer distance, which promote reversible potassium insertion and facilitate the charge transfer. Also, the calculated potassium diffusion coefficient during charge/discharge further proves the enhanced kinetics. Furthermore, The FeS2@NC anode in a full cell also exhibits high cyclic stability (88% capacity retention after 120 cycles with 99.9% Coulombic efficiency). Therefore, this work provides not only an approach to overcome several challenges in PIB anodes but also a comprehensive understanding of the mechanism and kinetics of the potassium interaction with chalcogenides.The (Fmes)BH2·SMe2 reagent (7) reacts sequentially with an acetylene and, e.g., xylylisonitrile in a convenient three-component reaction to give a series of unprecedented dihydro-1,3-azaborole derivatives 16. The tolane-derived example 16a was deprotonated and used as a ligand in organometallic chemistry. Compounds 16 served as the starting materials for the straightforward synthesis of various dihydro-1,3-azaborinine derivatives by treatment with an isonitrile. Several diaryldihydro-1,3-azaboroles showed interesting photophysical properties such as aggregation-induced emission and high fluorescence quantum yields.A cation substitution in Cu2ZnSn(S,Se)4 (CZTSSe) offers a viable strategy to reduce the open-circuit voltage (Voc)-deficit by altering the characteristics of band-tail states, antisite defects, and related defect clusters. Herein, we report a facile single process, i.e., simply introducing a thin Ag layer on a metallic precursor, to effectively improve the device characteristics and performances in kesterite (Agx,Cu1-x)2ZnSn(Sy,Se1-y)4 (ACZTSSe) solar cells. Probing into the relationship between the external quantum efficiency derivative (dEQE/dλ) and device performances revealed the Voc-deficit characteristics in the ACZTSSe solar cells as a function of Cu and Ag contents. The fabricated champion ACZTSSe solar cell device showed an efficiency of 12.07% and a record low Voc-deficit of 561 mV. Thorough investigations into the mechanism underpinning the improved performance in the ACZTSSe device further revealed the improved band-tailing characteristic, effective minority carrier lifetime, and diode factors as well as reduced antisite defects and related defect clusters as compared to the CZTSSe device. This study demonstrates the feasibility of effectively suppressing antisite defects, related defect clusters, and band-tailing characteristics by simply introducing a thin Ag layer on a metallic precursor in the kesterite solar cells, which in turn effectively reduces the Voc-deficit.Charge interaction-driven jamming of nanoparticle monolayers at the oil-water interface can be employed as a method to mold liquids into tailored stable 3D liquid objects. Here, 3D liquid objects are fabricated via a combination of biocompatible aqueous poly(vinyl sulfonic acid, sodium salt) solution and a colloidal dispersion of highly fluorescent organo-modified graphitic carbon nitride (g-C3N4) in edible sunflower oil. The as-formed liquid object shows stability in a broad pH range, as well as flexible pathways for efficient exchange of molecules at the liquid-liquid interphase, which allows for photodegradation of rhodamine B at the interface via visible light irradiation that also enables an encoding concept. The g-C3N4-based liquid objects point toward various applications, for example, all-liquid biphasic photocatalysis, artificial compartmentalized systems, liquid-liquid printing, or bioprinting.This work presents the synthesis of eight new rhodium(III) dihalido complexes, [RhX2(L)(LH)] (where X = Cl or I), which incorporate two bidentate N-(3-halidophenyl)picolinamide ligands. The ligands have different binding modes in the complexes, whereby one is neutral and bound via N,N (LH) coordination, while the other is anionic and bound via N,O (L) coordination. The solid state and solution studies confirm multiple isomers are present when X = Cl; however, after a halide exchange with potassium iodide (X = I) the complexes exist exclusively as single stable trans isomers. NMR studies reveal the Rh(III) trans diiodido complexes remain stable in aqueous solution with no ligand exchange reported over 96 h. Chemosensitivity data against a range of cancer cell lines show two cytotoxic complexes, where L = N-(3-bromophenyl)picolinamide ligand. The results have been compared to the analogous Ru(III) complexes and overall highlight the Rh(III) trans diiodido complex to be ∼78× more cytotoxic than the analogous Rh(III) dichlorido complex, unlike the Ru(III) complexes which are equitoxic against all cell lines. Additionally, the Rh(III) trans diiodido complex is more selective toward cancerous cells, with selectivity index (SI) values >25-fold higher than cisplatin against colorectal carcinoma.Separation or purification is one of the difficult problems in the petrochemical industry. To help solve the difficulty of separation or purification for C2H2/CO2 and C2Hn/CH4 in the chemical industry, we synthesized a new metal-organic framework (MOF), [Ni(dpip)]·2.5DMF·H2O (1), by a bipyridyl-substituted isophthalic acid ligand. The MOF includes two types of one-dimensional (1D) tubular channels with different sizes and porous environments. The unique tubular channels lead to not only remarkable gas sorption capacity of C2H4, C2H2, and CO2, but also good selectivity for C2H2/CH4, C2H2/CH4, CO2/CH4, and C2H2/CO2, as demonstrated by single-component sorption isotherm results, ideal adsorbed solution theory calculations, and dynamic breakthrough curves. Grand canonical Monte Carlo (GCMC) simulation reveals preferential adsorption sites in the MOF for CO2, C2H2, and C2H4. The MOF also exhibits an obvious size-selective absorption effect on vapor molecules.